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Clinical Study of perioperative goal-directed fluid therapy in pediatric neurosurgery

Clinical Study of perioperative goal-directed fluid therapy in pediatric neurosurgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16007731
Enrollment
Unknown
Registered
2016-01-09
Start date
2016-02-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric neurosurgery

Interventions

Traditional fluid therapy group:Empirical fluid therapy
Goal-directed fluid therapy group:PPV and continuous noninvasive hemoglobin monitoring guided goal-directed fluid therapy

Sponsors

Beijing Tiantan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 5 Years

Inclusion criteria

Inclusion criteria: Institutional approval and informed consent, ASA I-III, aged 18-80 years and weighed less than 20 kg, patients undergoing elective pediatric neurosurgery under general anesthesia, time in surgery more than 4 hours, no cardiopulmonary complications

Exclusion criteria

Exclusion criteria: Hyperpyrexia or hypothermia, emergency surgery, severe disfuction of vital organs, septicopyemia, expected survival time less than 1 year

Design outcomes

Primary

MeasureTime frame
Total postoperative complications within 15 days;—

Secondary

MeasureTime frame
Length of hospital stay;Fluid volume;Length of ICU stay;One-year mortality;Hemodynamic parameters;Brain relaxation;Blood gas analysis;—

Countries

China

Contacts

Public ContactXu Jin
xiehe2000@163.com+86 13693336261

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026